The role is transversal and supports CMC Quality Leads rather than being assigned permanently to a single product.
- Reviewing and assessing Material of Contact documentation, including extractables & leachables data and risk assessments.
- Supporting complaint committee activities, including trend analysis, data challenge, deviation follow-up and preparation of solid QA positioning.
- Contributing to process improvement strategies for complaint management, especially in preparation for FDA inspection.
- Drafting or reviewing QA documents, deviations and risk-based justifications
- Participating in meetings with internal stakeholders (mostly in English).
- Challenging incoming documentation on a daily basis and providing QA decisions.
- The role requires autonomy, strong critical thinking and the ability to operate in a non fully stabilized environment.